We have the team of quality experts who have experienced in formulation development, and method validation, stability programing, and also we have established parnetship with third party audit company & QC Lab in Mexico where we can provide extensive support to industry for their GMP audit of low risk molecule and local QC analysis. Also we support for preparation of COFEPRIS audit for high molecules/Products. Also athorised third party audit for low risk molecule/Products.
We also offered following services.
- Formulation development
- Technology transfer support
- Third party Lab analysis for batch release (Mexico and Brazil)
- Comparative Dissolution
- Preparation of SOP & STP's
